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Diabetic Foot UlcerNCT04564443

A Unique Micro Water Jet Technology Device Versus Standard Debridement in the Treatment of Diabetic Foot

A study testing Medaxis Debritom+, Sharp Surgical Debridement and Additional Outer Dressing Application in people with Diabetic Foot Ulcer and Diabetic Foot, run by Medaxis, LLC at 6 sites in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The purpose of this clinical investigation is to assess performance of the Medaxis Debritom+™ and to collect subject outcome data in the treatment of diabetic foot ulcers (DFU) vs Standard sharp debridement. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Diabetic Foot Ulcer, Diabetic Foot
What is being tested?
Medaxis Debritom+, Sharp Surgical Debridement and Additional Outer Dressing Application
Could I receive a placebo?
No, everyone receives an active treatment
How many people
222 participants
Where
6 sitesUnited States
Study dates
11 Sep 2020to 30 Dec 2024
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • At least 18 years old.
  • Presence of a diabetic foot ulcer (DFU) meets all of the following features: Wagner Grade 1 or 2 (see Appendix A for definitions), including wounds that extend to the ligament, tendon, joint capsule or fascia
  • At least 50% below the medial aspect of the malleolus
  • Without abscess or osteomyelitis
  • The index ulcer will be the largest ulcer if two or more DFUs are present and will be the only one evaluated in the study. If other ulcerations are present on the same foot, they must be more than 2 cm distant from the index ulcer.
  • The index ulcer (i.e. current episode of ulceration) has been present for greater than 4 weeks prior to SV1 and less than 1 year, as of the date the subject consents for study.
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  • The index ulcer is a minimum of 1.0 cm2 and a maximum of 25 cm2 at SV1 and TV1.
  • Adequate circulation to the affected foot as documented by a dorsal transcutaneous oxygen measurement (TCOM) or a skin perfusion pressure (SPP) measurement of ≥ 30 mmHg, or an Ankle Branchial Index (ABI) between 0.7 and 1.3 within 3 months of SV1, using the affected study extremity. As an alternative arterial Doppler ultrasound can be performed evaluating for biphasic dorsalis pedis and posterior tibial vessels at the level of the ankle within 3 months of SV1.
  • The index ulcer has been offloaded for at least 14 days prior to randomization.
  • Females of childbearing potential must be willing to use acceptable methods of contraception (birth control pills, IUD's, barriers or abstinence) during the course of the study and undergo pregnancy tests.
  • Subject understands and is willing to participate in the clinical study and can comply - with weekly visits.
  • Subjects must have read and signed the IRB approved ICF before screening procedures are undertaken.

Who cannot join

  • The index ulcer is deemed by the investigator to be caused by a medical condition other than diabetes.
  • The index ulcer, in the opinion of the investigator, is suspicious for cancer or has a positive carcinoma diagnosis.
  • Subjects with a history of more than two weeks of treatment with immune-suppressants (including systemic corticosteroids >10mg daily dose), cytotoxic chemotherapy, or application of topical steroids to the ulcer surface within 1-month prior to first SV1, or who receive such medications during the screening period or who are anticipated to require such medications during the course of the study.
  • Subjects taking a selective COX-2 inhibitor, such as Celecoxib, for any condition.
  • Subjects on any investigational drug(s) or therapeutic device(s) within 30 days preceding SV1.
  • History of radiation at the ulcer site (regardless of time since last radiation treatment).
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  • Index ulcer has been previously treated or will need to be treated with any prohibited therapies. (See Section 6.2.4 of this protocol for a list of prohibited medications and therapies).
  • Subjects with a previous diagnose of HIV, Hepatitis C, or other contagious diseases
  • Presence of any condition(s) which seriously compromises the subject's ability to complete this study or the subject has a known history of poor adherence with medical treatment.
  • Osteomyelitis or bone infection of the affected foot as verified by x-ray, CAT Scan, or MRI within 30 days prior to randomization. (In the event of an ambiguous diagnosis, the Principal Investigator will make the final decision).
  • Subject is pregnant or breast-feeding.
  • Presence of diabetes with poor metabolic control as documented with an HbA1c > 12.0 within 90 days of randomization.
  • Subjects with end stage renal disease as evidenced by a serum creatinine ≥ 3.0 mg/dL within 6 months of randomization.
  • Index ulcer has reduced in area by 20% or more after 14 days of SOC from SV1 to the TV1/randomization visit.

Trial locations and contacts

6 sites in 1 country.

6 sites in 1 country

United States6 sites
  • Foot and Ankle Associates of the Mid-Atlantic

    Frederick, Maryland, 21703

  • Foot and Ankle Associates of the Mid-Atlantic

    Raleigh, North Carolina, 27609

  • Foot and Ankle Associates of the Mid-Atlantic

    Salem, Virginia, 24153

  • CCR Research

    San Francisco, California, 94115

  • Doctors Research Network

    South Miami, Florida, 33143

  • Lower Extremity Institute for Research and Therapy, LLC

    Youngstown, Ohio, 44512

Other trials in United States

About this study

Official title: A Multi-center, Randomized Controlled Clinical Investigation Evaluating a Unique Micro Water Jet Technology Device Versus Standard Debridement in the Treatment of Diabetic Foot

The purpose of this clinical investigation is to assess performance of the Medaxis Debritom+™ and to collect subject outcome data in the treatment of diabetic foot ulcers (DFU) vs Standard sharp debridement.

Read the detailed description

The economic burden of DFUs costs the United States over $50 billion each year. The cost to treat one subject with DFUs ranges from $11,700 to $16,883. Although approximately 70% of DFUs are shown to heal with good SOC, at least 30% become chronic wounds. These non-healing wounds are at greater risk for infection and lower extremity amputation. Consequently, good standard of care therapy is important for subjects with chronic DFUs to improve subject outcomes, lower treatment costs and reduce the risk of complications.

The removal of necrotic tissue such as slough, eschar, and underlying biofilm constitutes one of the most important parts of standard of care (SOC). Currently, a variety of techniques are used to debride chronic wounds, such as larval therapy, autolytic and enzymatic methods, monofilament polyester fiber pads or brushes, and mechanical debridement with curettes and scalpels. It has also been demonstrated that more frequent debridement, on average, results in faster wound healing. While regarded as the "gold standard," sharp debridement requires considerable experience of clinicians to ensure that contaminated and devitalized tissue is entirely removed without extensively damaging surrounding healthy tissue. Moreover, a recent research has demonstrated that even when surgical debridement is well-conducted so that it removes the majority of biofilm, within 72 hours, biofilm often re-establishes itself. Given that perhaps 60% of chronic wounds have been found to harbor biofilm, it is challenging to keep such wounds free of biofilm so that the wound-healing process can be sustained. Consequently, any method that could potentially remove more biofilm and/or prevent its recurrence could improve the wound healing trajectory.

Medaxis Debritom+™ cleans and stimulates acute and chronic wounds precisely in a tissue-preserving manner. Its high-pressure micro fluid jet removes slough such as fibrin, necrosis or biofilm, as well as foreign bodies, in effect providing an efficient irrigation and debridement of contaminated wounds. The purpose of this clinical investigation is to assess performance of Medaxis Debritom+™ and to collect subject outcome data in the treatment of diabetic foot ulcers (DFU) vs Standard sharp debridement.

There are two arms in the study:

Arm 1: The Experimental Arm , that will include SOC Therapy. SOC therapy in this study is offloading of the DFU (CAM boots or total contact casting [TCC] if the subject's foot is too large for a CAM), use of the Medaxis Debritom+™ micro jet to clean the wound followed by a wound care covering ( Fibracol dressing or equivalent) along with a moisture retention dressing and a padded 3-layer dressing comprised of 4x4 gauze pads, soft roll and compression wrap (DynaflexTM or equivalent).

Arm 2: The Standard of Care Arm. The SOC therapy in this study is offloading of the DFU (CAM boots or total contact casting [TCC] if the subject's foot is too large for a CAM), appropriate sharp or surgical debridement, followed by a wound care covering (Fibracol dressing or equivalent) along with a moisture retention dressing and a padded 3-layer dressing comprised of 4x4 gauze pads, soft roll and compression wrap (DynaflexTM or equivalent).

Being tested
Medaxis Debritom+, Sharp Surgical Debridement, Additional Outer Dressing Application, Offloading, Fibracol Wound Dressing
Medical subject headings
Diabetic Foot

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Medaxis Debritom+Other

    Advanced micro fluid jet therapy to clean and stimulate wound

  • Sharp Surgical DebridementOther

    Scalpel or Curette to clean and debride wound

  • Additional Outer Dressing ApplicationOther

    Application of moisture retentive dressing, and a multi layer compression dressing

  • OffloadingOther

    Also called Pressure Relief

    Patient will be offloaded in a diabetic camboot after treatment, or total contact cast if patient cannot be fit with diabetic offloading boot

  • Fibracol Wound DressingOther

    Also called Calcium Alginate

    Application of a collagen alginate dressing

Study groups in NCT04564443
Study groupRoleWhat they receive
(Medaxis Debritom+™) micro fluid jet wound therapyExperimentalMedaxis Debritom+™ is a high-quality, micro fluid jet therapy device designed to remove fibrin, necrotic tissue, and biofilm from wound surfaces by mechanical cleaning and stimulation of the diabetic foot wound
Receives: Other: Medaxis Debritom+; Other: Additional Outer Dressing Application; Other: Offloading; Other: Fibracol Wound Dressing
Sharp Surgical DebridementActive comparatorUse of a surgical scalpel or curette to remove fibrin, necrotic tissue and biofilm from wound surfaces by mechanically cleaning the wound
Receives: Other: Sharp Surgical Debridement; Other: Additional Outer Dressing Application; Other: Offloading; Other: Fibracol Wound Dressing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of wounds completely healed at or before 16 weeks

    examine the time it takes the wound to heal over a 16 week period

    Measured: 16 weeks

Secondary outcomes (7)
  1. Incidence of any index wound-related cellulitis or infection by 16 weeks

    examine the number of subject that develop wound cellulitis or infection over 16 weeks

    Measured: 16 weeks

  2. Cost of treatment, including any index wound-related complications, by 16 weeks

    examine the cost of all treatments within 16 weeks

    Measured: 16 weeks

  3. Percent Area Reduction at 16 weeks.

    examine the reduction in wound size at 16 weeks

    Measured: 16 weeks

  4. Cost of hospitalization for any index wound-related event, including any wound recurrence involving the area of the index wound by 16 weeks

    examine the patient hospitalization costs for wound related event over 16 weeks

    Measured: 16 weeks

  5. Incidence of hospitalization between randomization and EOS for any index wound-related event, including any wound recurrence involving the area of the index wound

    examine the incidence of subject being hospitalized during the study period

    Measured: 16 weeks

  6. Moleculight imaging

    Difference in wound bioburden from wound biopsy

    Measured: 2 weeks

  7. Kent Imaging - Snapshot camera

    test oxygenation of wound tissue

    Measured: 16 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Sep 2020
  2. Study start11 Sep 2020
  3. Primary completion30 Dec 2024 (estimated)
  4. Study completion30 Dec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
222 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04564443
Sponsor's protocol ID
MEDX-DT-01
Status last verified
Nov 2024
First submitted
22 Sep 2020
Last updated
21 Nov 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Medaxis Debritom+, Sharp Surgical Debridement and Additional Outer Dressing Application in people with Diabetic Foot Ulcer and Diabetic Foot, run by Medaxis, LLC at 6 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 12 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 21 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of wounds completely healed at or before 16 weeks (time frame: 16 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Nov 2024.

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